N. Arsu et Rs. Davidson, PHOTOINITIATION OF ACRYLATE POLYMERIZATION BY 1-[4-(METHYLTHIO)PHENYL]-2-MORPHOLINO-PROPAN-1-ONE - SOME EFFECTS OF THE MORPHOLINO SUBSTITUENT, Journal of photochemistry and photobiology. A, Chemistry, 84(3), 1994, pp. 291-297
N-Isopropylmorpholine (IPM) was used as a model to investigate the pro
perties of the morpholino substituent present in 1-[4-(methylthio)phen
yl]-2-morpholino-propan-1-one (1). It was shown by real time IR (RTIR)
spectroscopy, photocalorimetry, bulk polymerization studies and the c
uring of thin films that IPM acts as a physical quencher for the tripl
et state of 1 and that it is a very poor hydrogen donor. Thus any inte
raction of the ground state of 1 with its triplet state is likely to l
ead to physical quenching, thereby reducing the initiating efficiency
of 1. Evidence is also presented that the use of high concentrations o
f N-methyldiethanolamine can lead to reduction of the triplet state of
1, thereby enhancing the initiating efficiency of 1. It was confirmed
that thioxanthones can sensitize the alpha cleavage of 1.